Selenium Injection (Arselenic Acid)
Selenious Acid 65.4μg
Injections · Prescription medication
Daehan Pharmaceutical Co., Ltd.
MFDS item code 201704564 · Notified 2017.06.22
Improvement of nutritional status through selenium supplementation
For patients receiving total parenteral nutrition (TPN), selenium supplementation is important. Selenium is an essential trace element that helps the body's antioxidant functions and immune function, and deficiency can lead to immune impairment or organ damage. Especially when using TPN, proper supplementation of selenium should be done to achieve nutritional balance and maintain overall health. Therefore, selenium supplementation during TPN treatment helps normalize bodily functions and prevent complications.
Inject 20 to 40 μg of selenium (this preparation contains 40 μg/mL of selenium) per day during stable metabolic total parenteral nutrition (TPN).
Inject 3 μg per kg of body weight per day.
This medication contains selenium and should not be used in patients with selenium toxicity. Toxicity may occur with overdose, so the medication should be discontinued immediately if symptoms appear. When administered intravenously, it should not be infused directly into peripheral veins without dilution; it must be diluted before administration. Use with caution in patients with poor kidney function or premature neonates, as there is a risk of aluminum accumulation with long-term parenteral administration. Rarely, pain or allergic reactions may occur during injection. If symptoms such as dermatitis, hair loss, or vomiting appear, consult a physician immediately. Before administration, ensure there are no precipitates or discoloration, and it must be prepared in a sterile state. In cases of kidney or gastrointestinal disorders, the selenium dosage should be adjusted, and in transfusion patients, the amount of selenium should also be considered. Women who are pregnant or may become pregnant should use this medication only when the benefits outweigh the risks to the fetus. For nursing mothers, as safety has not been established, it is recommended to discontinue breastfeeding or the medication. In cases of overdose, symptoms may include dermatitis, vomiting, metallic taste, and in severe cases, pulmonary hemorrhage or death, necessitating immediate treatment; there is no antidote and dialysis may be required. Store this medication in a sealed container away from air, in a cool place between 15 and 30 degrees Celsius, to maintain its effectiveness and safety.
Pain, allergic reactions (very rarely reported), dermatitis, odor during sweating and breathing, hair loss, irritability, vomiting, impact on nail and hair growth, oral abnormalities, gastrointestinal disturbances, tension, depression, metallic taste, garlic smell from the mouth.
Not everyone experiences these, and they can vary from person to person.
Store this medication in a sealed container to prevent air exposure, in a cool place between 15 and 30 degrees Celsius. This storage will maintain the medication's effectiveness and safety.
A colorless, odorless, transparent liquid contained in a colorless transparent glass vial injection.
10mL/vial
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.